ALUMINUM HYDROXIDE - Sunny Day Creations | Derma Care Research Labs, LLC

Manufacturer
Sunny Day Creations | Derma Care Research Labs, LLC
Effective date
2026-04-22
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:54:43

Label at a glance#

ProductLazy Face SPF 30 Facescreen
Active ingredientZINC OXIDE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide 2.3%, Zinc Oxide 4.8%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn. If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun.

WARNINGS SECTION

For external use only.

Do not use on damaged or broken skin.

When using this product avoid contact with eyes. Rinse with water to remove.

Stop use and ask a doctor if rash or irritation develops and lasts.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If product is swallowed, get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

For sunscreen use:
• Apply liberally 15 minutes before sun exposure and as needed
• Reapply:

• After 80 minutes of swimming or sweating • Immediately after towel drying
• At least every 2 hours

Sun protective measures

Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

• Limit time in the sun, especially from 10am–2pm. • Wear long-sleeved shirts, pants, hats, and

sunglasses
• Children under 6 months of age: ask a doctor

INACTIVE INGREDIENT SECTION

Water, C12-15 Alkyl Benzoate, Styrene/Acrylates Copolymer, Glycerin, Cetyl PEG/PPG-10/1 Dimethicone, Sorbitan Olivate, Dimethicone, Caprylic/Capric Triglyceride, C13-15 Alkane, Isononyl Isononanoate, Sodium Chloride, Acetyl Hexapeptide-8, Daucus Carota Sativa (Carrot) Root Extract, Tocopheryl Acetate, Beta-Carotene, Citrus Aurantium Dulcis (Orange) Peel Oil, Citrus Limon (Lemon) Peel Oil, Citrus Paradisi (Grapefruit) Peel Oil, Pelargonium Graveolens Flower Oil, Zingiber Officinale (Ginger) Root Oil, Ethylhexylglycerin, Benzyl Alcohol, Aluminum Starch Octenylsuccinate, Silica, Disodium EDTA, Polyhydroxystearic Acid, Triethoxycaprylylsilane, Aluminum Hydroxide, Stearic Acid, Phenoxyethanol

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-130850050802884GTIN-13: 0850050802884
EAN-13: 0850050802884
GTIN-12: 850050802884
UPC-A: 850050802884
GTIN storage (14 digits): 00850050802884
Lazyface_3oz Tube Carton_FINAL copy.jpg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87619-1869-3Lazy Face SPF 30 Facescreen1 in 1 CARTONLOTION11
87619-1869-3Lazy Face SPF 30 Facescreen85 g in 1 TUBELOTION851

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 33 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87619-186987619-1869-3

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 31 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lazy Face SPF 30 FacescreenTITANIUM DIOXIDE, ZINC OXIDESunny Day Creations500ee303-7302-68d5-e063-6394a90ac6d42026-04-22WarningsExact identifier
ndc (package): 87619-1869-3
ndc (product): 87619-1869
ndc11 (package): 87619186903
spl id: 500ee303-7303-68d5-e063-6394a90ac6d4
spl set id: 500ee303-7302-68d5-e063-6394a90ac6d4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.